Evidence map›Paper›PMID 40542048›Full record

ArticleScientific reports2025

A longitudinal analysis on alcohol consumption in patients with cancer undergoing psycho-oncological treatment.

Paulina Kiefer, Lisa Lebherz, Janina Freitag, Holger Schulz, Christiane Bleich, Carsten Bokemeyer, Frederike Bokemeyer

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Paulina Kiefer *Department of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany. p.kiefer@uke.de.
Lisa Lebherz *Department of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Janina FreitagDepartment of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Holger SchulzDepartment of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Christiane BleichDepartment of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Carsten BokemeyerCenter for Oncology, II. Medical Clinic and Polyclinic, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Frederike BokemeyerDepartment of Medical Psychology, University Medical Center Hamburg Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The negative impact of alcohol consumption on cancer development and progression is well-established in oncologic research, yet it receives surprisingly little attention from patients with cancer, the public, and even oncology professionals. A cancer diagnosis can lead to significant psychological distress, including high levels of depression and anxiety. For patients with cancer experiencing high levels of psychological burden, psycho-oncological care is available to help manage these symptoms and the overall impact of their condition. Alcohol consumption can serve as a coping mechanism for psychological stress. However, there is limited knowledge about the alcohol consumption patterns among this particularly vulnerable group of patients with cancer, as well as the patient- and disease-related factors associated with drinking. Patients with cancer are particularly susceptible to the harmful effects of alcohol. The aim of this study is to investigate the prevalence of potentially risky alcohol consumption among patients with cancer receiving psycho-oncological care over a six-month period and to identify sociodemographic, health-related, and psychosocial factors that may predict alcohol consumption after a cancer diagnosis. We conducted a secondary analysis using data from 300 patients with cancer (72 % female, mean age 52.74 years) treated at the outpatient clinic of the University Medical Center Hamburg-Eppendorf in Germany. Between 2013 and 2021 demographic, medical, and psychosocial information was collected using self-report questionnaires. A generalized longitudinal linear mixed model was used to determine the prevalence of risky and potentially harmful drinking behavior (AUDIT-C ≥ 2 for women and ≥ 3 for men) among patients with cancer as well as to identify patient characteristics associated with alcohol consumption. The results show that approximately 70% of the patients continued drinking after their cancer diagnosis, despite the known detrimental effects of alcohol on prognosis. At both time points, around 40 to 50% of female and male patients reported potentially harmful drinking behaviors (T0 (beginning of psychosocial treatment): 49.1% of female, 38.1% of male patients; T1 (6 months later): 41.2% of female and 42.9% of male patients). A higher number of comorbidities (OR = 0.707; 95% CI: 0.567-0.883), older age (OR = 0.983, 95% CI: 0.967-0.999, and higher levels of depressive symptoms (OR = 0.952, 95% CI: 0.907-0.998) were significantly associated with lower odds of risky alcohol consumption over the six-month period. In contrast, higher anxiety levels (OR = 1.075, 95% CI: 1.021-1.132) were associated with an increased likelihood of risky drinking. The significant proportion of patients with cancer consuming alcohol at levels that may worsen their cancer prognosis highlights the need for improved patient education and guidelines. The results can help identify high-risk patients who require close monitoring of their drinking behaviors during their survival period, and inform the implementation of better alcohol control measures in cancer care. By understanding alcohol consumption patterns and associated factors, we aim to promote healthier behaviors and improve treatment outcomes for patients with cancer in psycho-oncological care.

Indexed as

Alcohol DrinkingNeoplasmsAdultAgedAnxietyDepressionFemaleGermanyHumansLongitudinal StudiesMaleMiddle AgedPsycho-OncologyStress, PsychologicalSurveys and QuestionnairesAlcohol consumptionCancer survivorshipHealth behaviorsLifestyleLongitudinal analysisPsycho-oncologySupportive careTertiary prevention

Identifiers

PMID40542048
PMCPMC12181269

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.